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FDA 510(k)

FETAL/MATERNAL ALRM MODULE - 21595A

K-Number: K771194 · 1977-08-03

ApplicantHewlett-Packard Co.
Decision Date1977-08-03
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FETAL/MATERNAL ALRM MODULE - 21595A is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1977-08-03 under 510(k) number K771194. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FETAL/MATERNAL ALRM MODULE - 21595A?

FETAL/MATERNAL ALRM MODULE - 21595A is a medical device that received FDA 510(k) clearance on 1977-08-03. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K771194.

When did FETAL/MATERNAL ALRM MODULE - 21595A receive FDA 510(k) clearance?

FETAL/MATERNAL ALRM MODULE - 21595A received FDA 510(k) clearance on 1977-08-03, under 510(k) number K771194.

Who is the listed applicant for FETAL/MATERNAL ALRM MODULE - 21595A?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FETAL/MATERNAL ALRM MODULE - 21595A?

The FDA product code for FETAL/MATERNAL ALRM MODULE - 21595A is HGM.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: HGM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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